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Evis Exera Ii Bronchovideoscope

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
EVIS EXERA II BRONCHOVIDEOSCOPE FDA UDI
Generic Name
Flexible video bronchoscope, reusable FDA UDI
Device Name
BF-Q180 VIDEOSCOPE 5.1MM DIA 2.0MM CH FDA UDI
Model / Reference
OLYMPUS BF TYPE Q180 FDA UDI
Description
BF-Q180 VIDEOSCOPE 5.1MM DIA 2.0MM CH FDA UDI

Identifiers

Primary DI / UDI-DI
04953170339301 FDA UDI
FDA Product Code
EOQ FDA UDI
EOB FDA UDI
NWB FDA UDI
GMDN Term
Flexible video bronchoscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4680 FDA UDI
874.4760 FDA UDI
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible video bronchoscope, reusable

Evis Exera Ii Bronchovideoscope by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video bronchoscope, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI 25d11344-3302-4df6-9f47-4d75a533c59c 34 fields · synced May 30, 2026